| Product NDC: | 64809-104 |
| Proprietary Name: | Eyesaline Concentrate |
| Non Proprietary Name: | Water |
| Active Ingredient(s): | 92.2 mL/100mL & nbsp; Water |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 64809-104 |
| Labeler Name: | Sperian Eye & Face Protection Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part349 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110908 |
| Package NDC: | 64809-104-19 |
| Package Description: | 5323 mL in 1 BOTTLE, PLASTIC (64809-104-19) |
| NDC Code | 64809-104-19 |
| Proprietary Name | Eyesaline Concentrate |
| Package Description | 5323 mL in 1 BOTTLE, PLASTIC (64809-104-19) |
| Product NDC | 64809-104 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Water |
| Dosage Form Name | LIQUID |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20110908 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Sperian Eye & Face Protection Inc. |
| Substance Name | WATER |
| Strength Number | 92.2 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |